Site Selection Lead

Develop, in conjunction with the Global Feasibility Lead, the initial site list for feasibility and site identification
Full oversight of the Feasibility/Site identification process: survey development and programming, local resource training and oversight, oversight of site outreach process, creation of progress reports, site selection tool and decision making, customer interaction
Collaborate with Global Feasibility Leads to support collection of country and investigator feedback in the pre-award space; provide summary and analysis of results
Responsible for setup and conduct for feasibility/site identification studies according to timeline and quality standards and client expectations
Develop site lists according to the program or protocol:
Work closely with Global Feasibility Lead, strategy, and start up teams to understand optimal site profile
Evaluate the available sources of potential site information, and the pros and cons of each.
Manage timelines and any changes to the target site list requirements up until the site is fully identified and the target number of potential sites in each defined region and country is achieved.
Helping to facilitate identity matching by coordinating the triggers for master data management
Perform literature and internet searches as required.
Learn and utilize the data sources available for site performance data.
Create electronic surveys using company software and produce any required standalone or topline surveys
Participate in internal planning meetings and contributes during client interactions and interim teleconferences.
Ensure accuracy and quality of survey driven data
Work with team and other Senior staff to identify potential risks and out of scope activity; discusses contingency plans with stakeholders as appropriate.
Ensure site identification team in each country is entering and updating internal tracking tools.
Develop and deliver training of feasibility and site identification requirements/processes
Liaise with the global, cross-functional teams, inclusive of legal, start-up, clinical, country teams, and project management.
Participates in the development, implementation, and maintenance of systems.
Contribute to audit presentations/documentation based on site ID oversight
Performs any other duties as assigned

Minimum required:

Minimum 3-5 years of clinical research experience in pharmaceutical company/ CRO or other equivalent experience with increasing level of responsibility in site selection, site identification and feasibility along with strong excel skills.

Education/Qualification - University/ college degree (life science preferred) from an appropriately accredited institution.

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